BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

377 related articles for article (PubMed ID: 25995800)

  • 1. Cutis Laxa syndrome: a case report.
    Hbibi M; Abourazzak S; Idrissi M; Chaouki S; Atmani S; Hida M
    Pan Afr Med J; 2015; 20():3. PubMed ID: 25995800
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Cutis laxa syndrome. Case report].
    Kermane A; Tachfouti S; Lezrek M; Mohcine Z
    Bull Soc Belge Ophtalmol; 2004; (292):5-8. PubMed ID: 15253484
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Congenital cutis laxa: a case study].
    El Ouali A; Azizi M; Dikhaye S; Benajiba N
    Pan Afr Med J; 2019; 34():195. PubMed ID: 32180869
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal recessive form of congenital cutis laxa: more than the clinical appearance.
    Andiran N; Sarikayalar F; Saraçlar M; Cağlar M
    Pediatr Dermatol; 2002; 19(5):412-4. PubMed ID: 12383097
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Congenital generalized cutis laxa].
    Lambert D; Beer F; Jeannin-Magnificat C; Mabille JP; Israël J; Lambert-Weyl M; Nivelon-Chevalier A; Alison M
    Ann Dermatol Venereol; 1983; 110(2):129-38. PubMed ID: 6881855
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Congenital generalized cutis laxa: 5 cases].
    Rybojad M; Baumann C; Godeau G; Moraillon I; Prigent F; Morel P; Bourrat E
    Ann Dermatol Venereol; 1999 Apr; 126(4):317-9. PubMed ID: 10421933
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bilateral congenital entropion with cutis laxa.
    Al-Faky YH; Salih MA; Mubarak M; Al-Rikabi AC
    Pediatr Dermatol; 2014; 31(3):e82-4. PubMed ID: 24517732
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Cutis laxa syndrome. Clinical, histologic and ultrastructural study of a new variant].
    Pitzalis G; Bonamico M; Mariani P; Palmieri G; Ceccamea A; Signoretti A
    Minerva Pediatr; 1989 Apr; 41(4):193-7. PubMed ID: 2770644
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Defective protein glycosylation in patients with cutis laxa syndrome.
    Morava E; Wopereis S; Coucke P; Gillessen-Kaesbach G; Voit T; Smeitink J; Wevers R; Grünewald S
    Eur J Hum Genet; 2005 Apr; 13(4):414-21. PubMed ID: 15657616
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cutis laxa of the autosomal recessive type in a consanguineous family.
    de Schepper S; Loeys B; de Paepe A; Lambert J; Naeyaert JM
    Eur J Dermatol; 2003; 13(6):529-33. PubMed ID: 14721770
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital cutis laxa syndrome: type II autosomal recessive inheritance.
    Tüysüz B; Arapoğlu M; Ilikkan B; Demirkesen C; Perk Y
    Turk J Pediatr; 2003; 45(3):265-8. PubMed ID: 14696810
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital cutis laxa.
    Oku T; Nakayama F; Imaizumi S; Takigawa M; Yamada M
    Dermatologica; 1989; 179(2):79-83. PubMed ID: 2792495
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Acquired cutis laxa type II (Marshall syndrome) in an 18-month-old child: a case report.
    Haider M; Alfadley A; Kadry R; Almutawa A
    Pediatr Dermatol; 2010; 27(1):89-91. PubMed ID: 20199420
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal recessive cutis laxa syndrome. A case report.
    Jung K; Ueberham U; Hausser I; Bosler K; John B; Linse R
    Acta Derm Venereol; 1996 Jul; 76(4):298-301. PubMed ID: 8869689
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cutis laxa, congenital form with pulmonary emphysema: an ultrastructural study.
    Ledoux-Corbusier M
    J Cutan Pathol; 1983 Oct; 10(5):340-9. PubMed ID: 6630666
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica.
    Kariminejad A; Afroozan F; Bozorgmehr B; Ghanadan A; Akbaroghli S; Khorram Khorshid HR; Mojahedi F; Setoodeh A; Loh A; Tan YX; Escande-Beillard N; Malfait F; Reversade B; Gardeitchik T; Morava E
    Int J Mol Sci; 2017 Mar; 18(3):. PubMed ID: 28294978
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
    Morava E; Lefeber DJ; Urban Z; de Meirleir L; Meinecke P; Gillessen Kaesbach G; Sykut-Cegielska J; Adamowicz M; Salafsky I; Ranells J; Lemyre E; van Reeuwijk J; Brunner HG; Wevers RA
    Eur J Hum Genet; 2008 Jan; 16(1):28-35. PubMed ID: 17971833
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Cutis laxa. Classification, clinical aspects and molecular defects].
    Mensing H; Krieg T; Meigel W; Braun-Falco O
    Hautarzt; 1984 Oct; 35(10):506-11. PubMed ID: 6500933
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A case of congenital cutis laxa (generalized elastolysis).
    Champion P; Ryan F
    Can Respir J; 2005 Apr; 12(3):151-2. PubMed ID: 15875069
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Generalized cutis laxa associated with heavy chain deposition disease.
    Tan S; Pon K; Bargman J; Ghazarian D
    J Cutan Med Surg; 2003; 7(5):390-4. PubMed ID: 14973644
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.